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Carcinoid Tumor

More information in Books or onNLM PubMed
Definition: A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182)  /blood supply /chem /second /secret /ultrastruct permitted; coord IM with precoord organ/neopl term (IM); consider also MALIGNANT CARCINOID SYNDROME or CARCINOID HEART DISEASE   
Examples Malignant Carcinoid Syndrome
Other names Carcinoid, Goblet Cell; Carcinoid; Argentaffinoma; Tumors, Carcinoid; Tumor, Carcinoid; Goblet Cell Carcinoids; Goblet Cell Carcinoid; Carcinoids, Goblet Cell; Carcinoids; Carcinoid Tumors; Argentaffinomas
 
SubstanceCAS Registry & nameCategoriesSource
chromogranin A-derived peptide, WE-14  115136-18-0   *Neoplasm Proteins *Chromogranin A Carcinoid Tumor Chromogranins. FEBS Lett 1992 Apr 27;301(3):319-21

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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